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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526835Generated: October 27, 2026

Toluene → 6-Bromo-4-chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinoline

https://huagongshe.com/reaction/526835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAluminumHCID 5359268—
ReactantSodium MethoxideHCID 10942334—
Reactant6-Bromo-2,4-dichloro-3-(4-(trifluoromethyl)benzyl)quinolineHCID 86715628—
SolventMethylenechloride HexaneHCID 21226440—
Product6-Bromo-4-chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolineHCID 86715627—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 1 L flask containing 6-bromo-2,4-dichloro-3-(4-(trifluoromethyl)benzyl)quinoline (32.5 g, 74.7 mmol, Intermediate 5: step c) was added toluene (550 mL) followed by solid sodium methoxide (40 g, 740 mmol, 97% purity) at room temperature. The suspension was stirred at reflux (˜118° C.) in an aluminum mantle. TLC (50% hexane-DCM) and HPLC after 5.5 hours showed the reaction to be complete. The reaction mixture was filtered through Celite® while still warm (˜80° C.) and rinsed with warm toluene (˜70° C., 500 mL). The colorless filtrate was concentrated which then solidified to afford the title compound as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346782B2
Source datasetuspto-grants-2016_05
ORD IDord-d17bbea1afb0401bbb779c9c475c1fe3
Source noteuspto-grants-2016_05